3-Glycyl-2-phenyl-4-thiazolidinecarboxylic acid ethyl ester hydrobromide

Base Information

Chemical Name:3-Glycyl-2-phenyl-4-thiazolidinecarboxylic acid ethyl ester hydrobromide
CAS No.:107321-80-2
Molecular Formula:BrH*C₁₄H₁₈N₂O₃S
Molecular Weight:375.286
Hs Code.:
DSSTox Substance ID:DTXSID80910294

Synonyms:3-Glycyl-2-phenyl-4-thiazolidinecarboxylic acid ethyl ester hydrobromide;Ethyl-2-phenyl-3-glycylthiazolidine-4-carboxylate hydrobromide;4-Thiazolidinecarboxylic acid, 3-glycyl-2-phenyl-, ethyl ester, hydrobromide;4-Thiazolidinecarboxylic acid, 3-(aminoacetyl)-2-phenyl-, ethyl ester, monohydrobromide;107321-80-2;C14H18N2O3S.BrH;DTXSID80910294;C14-H18-N2-O3-S.Br-H;LS-151193;Ethyl 3-glycyl-2-phenyl-1,3-thiazolidine-4-carboxylate--hydrogen bromide (1/1)

Suppliers and Price of 3-Glycyl-2-phenyl-4-thiazolidinecarboxylic acid ethyl ester hydrobromide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 3-Glycyl-2-phenyl-4-thiazolidinecarboxylic acid ethyl ester hydrobromide

Chemical Property:

Vapor Pressure:1.63E-09mmHg at 25°C
Boiling Point:483.7°Cat760mmHg
Flash Point:246.4°C
Density:g/cm³
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:5
Exact Mass:374.02998
Heavy Atom Count:21
Complexity:358

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)C1CSC(N1C(=O)CN)C2=CC=CC=C2.Br

Technology Process of 3-Glycyl-2-phenyl-4-thiazolidinecarboxylic acid ethyl ester hydrobromide

There total 2 articles about 3-Glycyl-2-phenyl-4-thiazolidinecarboxylic acid ethyl ester hydrobromide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 56.0%

: 107321-72-2
(R)-3-(2-Benzyloxycarbonylamino-acetyl)-2-phenyl-thiazolidine-4-carboxylic acid ethyl ester

: 107321-80-2
ethyl-2-phenyl-3-glycylthiazolidine-4-carboxylate hydrobromide

Guidance literature:: With hydrogen bromide; Ambient temperature;

Reference yield:

: 189228-43-1
(2RS,4R)-2-phenylthiazolidine-4-carboxylic acid ethyl ester

: 107321-80-2
ethyl-2-phenyl-3-glycylthiazolidine-4-carboxylate hydrobromide

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine; isobutylchloroformate / 1.) THF, -15 deg C, 3 h; 2.) rt, 20-24 h

2: 56 percent / hydrogen bromide in acetic acid / Ambient temperature

With hydrogen bromide; triethylamine; isobutyl chloroformate;